ライフサイエンスコーパス: neonatal diabetes mellitus

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1 ns associated with beta-cell dysfunction and neonatal diabetes mellitus.

2 Mutations that impair folding cause neonatal diabetes mellitus.

3 in secretion as the major cause of permanent neonatal diabetes mellitus.

4 is of the spectrum of disorders constituting neonatal diabetes mellitus.

5 gression of disease states such as transient neonatal diabetes mellitus.

6 ld be tested for in adults with a history of neonatal diabetes mellitus.

7 expressed gene or genes that cause transient neonatal diabetes mellitus.

8 lso be considered in patients with transient neonatal diabetes mellitus.

9 with fetal growth retardation and transient neonatal diabetes mellitus.

10 To date, all patients with transient neonatal diabetes mellitus and uniparental disomy have h

11 for rarely occurring transient and permanent neonatal diabetes mellitus, and transgenic animal models

12 chromosome 10p13-p12.1 involved in permanent neonatal diabetes mellitus associated with pancreatic an

13 types in a cohort of patients diagnosed with neonatal diabetes mellitus before age 1 year, without be

14 utations (Y330C, F333I) that cause permanent neonatal diabetes mellitus, by heterologous expression i

15 ions, Y330C and F333I, which cause permanent neonatal diabetes mellitus, disrupt this motif and abrog

16 ently, a transgenic mouse model of transient neonatal diabetes mellitus due to mutations in ZAC/HYMAI

17 A new mouse model of transient neonatal diabetes mellitus emphasizes that both the numb

18 To determine whether human X-linked neonatal diabetes mellitus, enteropathy and endocrinopat

19 Transient neonatal diabetes mellitus has been associated with abno

20 Neonatal diabetes mellitus is a rare genetic form of pan

21 Neonatal diabetes mellitus is often associated with neur

22 Although neonatal diabetes mellitus is rare, its molecular basis

23 Neonatal diabetes mellitus (NDM) can be caused by gain-o

24 This was demonstrated in a murine model of Neonatal Diabetes Mellitus (NDM) involving expression of

25 Neonatal diabetes mellitus (NDM) is a rare form of diabe

26 Remission of neonatal diabetes mellitus occurred in 89 (51%) index pa

27 molecular mechanisms underlying permanenent neonatal diabetes mellitus (PNDM) in a patient with a he

28 (+) channel (K(ATP) channel) cause permanent neonatal diabetes mellitus (PNDM) in humans.

29 n the insulin (INS) gene may cause permanent neonatal diabetes mellitus (PNDM).

30 nts from 20 countries referred to the French Neonatal Diabetes Mellitus Study Group from 1995 to 2010

31 Transient neonatal diabetes mellitus (TNDM) is a rare disease char

32 Transient neonatal diabetes mellitus (TNDM) is a rare disorder ass

33 Transient neonatal diabetes mellitus (TNDM) is a rare form of chil

34 Transient neonatal diabetes mellitus (TNDM) is associated with int

35 Transient neonatal diabetes mellitus (TNDM) is diagnosed in the fi

36 ted the localization of a gene for transient neonatal diabetes mellitus (TNDM), a rare form of childh

37 eved to underlie the rare disorder transient neonatal diabetes mellitus (TNDM).

38 Individuals with permanent neonatal diabetes mellitus usually present within the fi

39 duce the sensitivity of ATP inhibition cause neonatal diabetes mellitus via suppression of beta-cell

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